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Kathrin Hauser

Showing results (1-10 of 52) with videos related to

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Praxis|October 18, 2012
[Gestational diabetes]Kathrin Hauser, Daniel Franzen, Roger Lehmann
Parkinsonism & Related Disorders|July 25, 2016
Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variantMax Güldner, Claudia Schulte, Ann-Kathrin Hauser, et al.
Neurobiology of Aging|January 19, 2016
Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's diseaseRichard Wüst, Brigitte Maurer, Kathrin Hauser, et al.
Anesthesia and Analgesia|October 24, 2006
The effects of dexmedetomidine/remifentanil and midazolam/remifentanil on auditory-evoked potentials and electroencephalogram at light-to-moderate sedation levels in healthy subjectsMatthias Haenggi, Heidi Ypparila, Kathrin Hauser, et al.
Critical Care (London, England)|February 21, 2009
Intra- and inter-individual variation of BIS-index and Entropy during controlled sedation with midazolam/remifentanil and dexmedetomidine/remifentanil in healthy volunteers: an interventional studyMatthias Haenggi, Heidi Ypparila-Wolters, Kathrin Hauser, et al.
Microbiology Resource Announcements|May 27, 2021
Draft Genome Sequences of Two Listeria monocytogenes Strains Isolated from Invasive Snails (Arion vulgaris) in Austria in 2019Ariane Pietzka, Andrea Murer, Anna Lennkh, et al.
Parkinsonism & Related Disorders|October 18, 2015
Neurodegenerative CSF markers in genetic and sporadic PD: Classification and prediction in a longitudinal studyKathrin Brockmann, Claudia Schulte, Christian Deuschle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 3, 2014
GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal studyKathrin Brockmann, Karin Srulijes, Sylvia Pflederer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2013
SNCA: major genetic modifier of age at onset of Parkinson's diseaseKathrin Brockmann, Claudia Schulte, Ann-Kathrin Hauser, et al.
Journal of Neurology|May 11, 2015
Clinical variability in ataxia-telangiectasiaEbba Lohmann, Stefanie Krüger, Ann-Kathrin Hauser, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Praxis|October 18, 2012
[Gestational diabetes]Kathrin Hauser, Daniel Franzen, Roger Lehmann
Parkinsonism & Related Disorders|July 25, 2016
Broad clinical phenotype in Parkinsonism associated with a base pair deletion in RAB39B and additional POLG variantMax Güldner, Claudia Schulte, Ann-Kathrin Hauser, et al.
Neurobiology of Aging|January 19, 2016
Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's diseaseRichard Wüst, Brigitte Maurer, Kathrin Hauser, et al.
Anesthesia and Analgesia|October 24, 2006
The effects of dexmedetomidine/remifentanil and midazolam/remifentanil on auditory-evoked potentials and electroencephalogram at light-to-moderate sedation levels in healthy subjectsMatthias Haenggi, Heidi Ypparila, Kathrin Hauser, et al.
Critical Care (London, England)|February 21, 2009
Intra- and inter-individual variation of BIS-index and Entropy during controlled sedation with midazolam/remifentanil and dexmedetomidine/remifentanil in healthy volunteers: an interventional studyMatthias Haenggi, Heidi Ypparila-Wolters, Kathrin Hauser, et al.
Microbiology Resource Announcements|May 27, 2021
Draft Genome Sequences of Two Listeria monocytogenes Strains Isolated from Invasive Snails (Arion vulgaris) in Austria in 2019Ariane Pietzka, Andrea Murer, Anna Lennkh, et al.
Parkinsonism & Related Disorders|October 18, 2015
Neurodegenerative CSF markers in genetic and sporadic PD: Classification and prediction in a longitudinal studyKathrin Brockmann, Claudia Schulte, Christian Deuschle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 3, 2014
GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal studyKathrin Brockmann, Karin Srulijes, Sylvia Pflederer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 16, 2013
SNCA: major genetic modifier of age at onset of Parkinson's diseaseKathrin Brockmann, Claudia Schulte, Ann-Kathrin Hauser, et al.
Journal of Neurology|May 11, 2015
Clinical variability in ataxia-telangiectasiaEbba Lohmann, Stefanie Krüger, Ann-Kathrin Hauser, et al.
Pageof 6